Journals / Medicine Science / 2016 / Cilt: 5 - Sayı: 2

Protective effects of melatonin and B-D-glucan against acetaminophen toxicity in rats

Pages
539–543
DOI
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⚡ TL;DR(Too Long; Didn't Read)

We concluded that combination of melatonin and ?-D-glucan may be attributed to scavenging free radicals and stimulating the antioxidant enzymes.

📌 3 Key Takeaways

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Objective & Hypothesis:The aim of this study was to investigate the possible protective effects of melatonin and ?-D-glucan against AA-induced liver injury in rats.
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Key Findings & Data:Forty (Spraque-Dawley male) rats were randomly divided into 5 experimental groups: sham (S), acetaminophen only (AA, 900 mg/kg), melatonin (10 mg/kg) + AA (MLT), ?D-glucan (50 mg/kg) + AA (?), and melatonin + ?-D-glucan + AA (MLT+?) groups.
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Conclusion & Impact:We concluded that combination of melatonin and ?-D-glucan may be attributed to scavenging free radicals and stimulating the antioxidant enzymes.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The aim of this study was to investigate the possible protective effects of melatonin and ?-D-glucan against AA-induced liver injury in rats. Forty (Spraque-Dawley male) rats were randomly divided into 5 experimental groups: sham (S), acetaminophen only (AA, 900 mg/kg), melatonin (10 mg/kg) + AA (MLT), ?D-glucan (50 mg/kg) + AA (?), and melatonin + ?-D-glucan + AA (MLT+?) groups. All of the rats were killed on day 11 of the experiment. Histopathological changes and biochemical parameters including levels of serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) and liver tissue malondialdehyde (MDA), activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) were determined to assess the liver function. MDA levels were the highest in the AA group whereas activities of SOD, CAT, and GPx in the liver tissue were found as lowest in this group. MDA activities were significantly lower in the MLT+? group than in the AA group. Only GPx activities in the MLT+? group were significantly higher than those in the MLT and ? groups. The serum AST and ALT levels were increased significantly following treatment with AA (p < 0.001). Pretreatment with the antioxidant compounds decreased AST levels significantly but again, the levels were still significantly higher than the sham levels (p < 0.001). There were no statistically significant differences in the microscopic damage between the S, MLT, ?, and MLT+? groups (p > 0.05). We concluded that combination of melatonin and ?-D-glucan may be attributed to scavenging free radicals and stimulating the antioxidant enzymes.

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Cite This Article

AYDOĞAN, M. S., POLAT, A., VARDI, N., ERDOĞAN, M. A., YÜCEL, A., YILDIZ, A., ÖZGÜL, Ü., UÇAR, M., ÇOLAK, C. (2016). Protective effects of melatonin and B-D-glucan against acetaminophen toxicity in rats. Medicine Science, Cilt: 5 - Sayı: 2, 539–543. https://ajindex.com/articles/277535

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References (15)

  1. Sener G, Sehirli AO, Ayanoğlu G. Protective effects of melatonin, vitamin E and N-acetylcysteine against acetaminophen toxicity in mice: a comparative study. J Pineal Res. 2003;35:61-8
  2. Gu J, Cui H, Behr M, Zhang L. In vivo mechanisms of tissueselective drug toxicity: effects of liver-specific knockout of the NADPH-cytochrome P-450 reductase gene on acetaminophen toxicity in kidney, lung, and nasal mucosa. Mol Pharmacol. 2005;67:623-30
  3. Zaher H, Buters JT, Ward JM, Bruno MK. Protection against acetaminophen toxicity in CYP1A2 and CYP2E1 double-null mice. Toxicol Appl Pharmacol. 1998;152:193-9
  4. Ilbey YO, Ozbek E, Cekmen M, Somay A. Melatonin prevents acetaminophen-induced nephrotoxicity in rats. Int Urol Nephrol 2009;41:695-702
  5. Reiter RJ, Tan DX, Manchester LC, Qi W. Biochemical reactivity of melatonin with reactive oxygen and nitrogen species. Cell Biochem Biophys. 2001;34:237-56
  6. Lake BG, Harris RA, Phillips JC, Gangolli S. D. Studies on the effects of L-ascorbic acid on acetaminophen-induced hepatotoxicity
  7. Inhibition of the covalent binding of acetaminophen metabolites to hepatic microsomes in vitro. Toxicol Appl Pharmacol. 1981;60:229- 40
  8. Toklu HZ, Sener G, Jahovic N, Uslu B. Beta-glucan protects against burn-induced oxidative organ damage in rats. Int Immunopharmacol. 2006;6:156-69
  9. Krizková L, Duracková Z, Sandula J, Slamenová D,Sasinková V, Sivonová M, Krajcovic J. Fungal beta-(1-3)-D-glucan derivatives exhibit high antioxidative and antimutagenic activity in vitro. Anticancer Res. 2003;23:2751-6
  10. Babincová M, Bacová Z, Machová E, Kogan G. Antioxidant properties of carboxymethyl glucan: comparative analysis. J Med Food. 2002;5:79-83
  11. Toklu HZ, Sehirli AO, Velioğlu-Oğünç A, Cetinel S. Acetaminophen-induced toxicity is prevented by beta-D-glucan treatment in mice. Eur J Pharmacol. 2006;14;543:133-40
  12. Parlakpinar H, Sahna E, Ozer MK, Ozugurlu. Physiological and pharmacological concentrations of melatonin protect against cisplatin-induced acute renal injury. J Pineal Res. 2002;33:161-6
  13. Aydogan MS, Yucel A, Erdogan MA, Polat A, Cetin A, Ucar M, Duran ZR, Durmus M. "Effects of ?-glucan on liver ischemia/reperfusion injury in rats", Transplantation Proceedings. 2013;45(2):487-91
  14. Aydogan MS, Erdogan MA, Polat A, Yücel A, Ozgül U, Parlakpinar H, Duran ZR, Yildiz A, Durmus M, "Effects of melatonin and ?- glucan combination hepatic ischemia and reperfusion in rats". Adv Clin Exp Med. 2013;22(5);621-7
  15. Kanno